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UnknownIntegrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.
Not available
S-EPMC4338501 | biostudies-literature
UnknownThe functional spectrum of low-frequency coding variation.
Not available
S-EPMC3308047 | biostudies-literature
UnknownA global reference for human genetic variation.
Not available
S-EPMC4750478 | biostudies-literature
UnknownDiversity of human copy number variation and multicopy genes.
Not available
S-EPMC3020103 | biostudies-literature
UnknownThe 1000 Genomes Project: data management and community access.
Not available
S-EPMC3340611 | biostudies-literature
UnknownDemographic history and rare allele sharing among human populations.
Not available
S-EPMC3142009 | biostudies-literature
UnknownA map of human genome variation from population-scale sequencing.
Not available
S-EPMC3042601 | biostudies-literature
UnknownMapping copy number variation by population-scale genome sequencing.
Not available
S-EPMC3077050 | biostudies-literature
UnknownIntegrative annotation of variants from 1092 humans: application to cancer genomics.
Not available
S-EPMC3947637 | biostudies-literature
UnknownHuman genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences.
Not available
S-EPMC4197830 | biostudies-literature
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